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Register to vote Register by 18 June to vote in the General Election on 4 July.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Guide for overseas investors on how to access NHS procurement channels.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
Batches of some products made by Legency Remedies Pvt Ltd have been found to contain a bacteria called Ralstonia pickettii (R. pickettii). All potentially affected batches are being recalled following an MHRA investigation.
Batches of Legency Remedies Pvt Ltd irrigation, inhalation and eye wash saline products manufactured between April and November 2023 are being recalled due to potential microbiological contamination.
The Medicines and Healthcare products Regulatory Agency (MHRA), working with law enforcement partners, seized more than 15.5 million doses of illegally traded medicines with a street value of more than £30 million during 2023.
How investigators and sponsors should manage clinical trials during COVID-19
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to prepare for implementation and compliance of the Safety Features Regulation.
Desitin Pharma UK Ltd is recalling all batches of Lamotrigine Desitin 10mg/ml Oral Suspension as a precautionary measure due to an out of specification observation in the appearance of samples during routine stability testing. Please note this is a Class...
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
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